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Journal of Medical Genetics|March 21, 1998
Beckwith-Wiedemann syndrome in a child with chromosome 18q deletionC M Brewer, W W Lam, C Hayward, et al.
Journal of Internal Medicine|July 29, 1998
Molecular genetic analysis of von Hippel-Lindau diseaseF M Richards, A R Webster, R McMahon, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|February 16, 2021
Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies: Scientific Impact Paper No. 64 [February] 2021F Mone, D J McMullan, D Williams, et al.
British Journal of Cancer|November 10, 2004
Epigenetic inactivation of SLIT3 and SLIT1 genes in human cancersR E Dickinson, A Dallol, I Bieche, et al.
Peptides|August 22, 2001
Adrenomedullin expression in pathogen-challenged oral epithelial cellsS Kapas, A Bansal, V Bhargava, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1988
Captopril-enhanced 99mTc DTPA scintigraphy in the detection of renal-artery stenosisE R Maher, S Othman, A H Frankel, et al.
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